HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-N-Boc-4-N-Methyl-aminopiperidine → HCID 131721052, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-N-Boc-4-N-Methyl-aminopiperidine | HCID 2756806 | — |
| Reactant | 5-bromo-1,1-dimethoxypentane | HCID 11074684 | — |
| Product | HCID 131721052 | HCID 131721052 | — |
Reaction Steps
The title compound was prepared from the above amine and 5-bromopentanal dimethyl acetal using a similar method to that described for Example 8 (Step 2). δ (360 MHz, CDCl3) 1.34 (1H, m), 1.46-1.73 (19H, m and s), 1.98 (2H, m), 1.33 (2H, m), 2.73 (3H, s), 2.99 (2H, m), 3.31 (6H, s), 4.36 (1H, t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05854268 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-459f5754eee0492f989e17eba5cbd9a0 |
| Source note | uspto-grants-1998_12 |